This workshop has been developed to provide overview of clinical research process with a comprehensive review of ICH GCP, USFDA CFR 21, Schedule Y and the elements involved in coordinating a clinical trial.
Who Should Attend?
· Medicine / Life Sciences / Science Graduates & Post Graduates & Students.
· Entry level & Junior CRCs, CRAs and other clinical research professionals with limited experience.
· Anyone interested in the field of clinical research.
Following topics will be covered during the workshop by industry experts :
· Fundamentals of Clinical Research
· Ethical Concerns and Human Subject Protection
· Regulatory Issues
· Subject Recruitment & Retention
· Conduct of Clinical Trials
· Adverse Event Reporting
Course Objectives : Upon completion of the workshop, the attendee should be able to understand the clinical research fundamentals, conduct and management of clinical trials, ethical issues and regulatory issues.
Dates of Workshop : 15-16 March 2008 (Saturday & Sunday) - Timings : 9 a.m. to 5 p.m.
Last Date of Registration : 13th March 2008. Limited seats available.
Registration Fee : Rs.4,500/-
Payment Mode : By Cash or Bank Draft/Cheque favouring `Tenet Health Edutech Pvt. Ltd., payable at New Delhi.
Workshop Venue : Cliniminds, C-55 First Floor, Preet Vihar, Main Vikas Marg, Delhi 110092
Certificates: Certificates of Participation will be issued to all participants.
For Registration & Information Please Contact
Cliniminds
C-55 First Floor, Preet Vihar,
Main Vikas Marg, Delhi 110092
Mobile : 9871072560; 9810068241; 9999851016;
Email : info@cliniminds. com; Website : www.cliniminds. com
